Align L-lactate dehydrogenase iron-sulfur cluster-binding protein LldF (characterized, see rationale)
to candidate Dsui_0126 Dsui_0126 (4Fe-4S) cluster-containing protein
Query= uniprot:Q8EGS5 (464 letters) >FitnessBrowser__PS:Dsui_0126 Length = 479 Score = 311 bits (796), Expect = 4e-89 Identities = 169/433 (39%), Positives = 247/433 (57%), Gaps = 17/433 (3%) Query: 46 AAGSLPEWEQLRQLGSEIKLHTLTNLAQYLETFEQNCLANGIKVHWAKDGAEHNRIVHEI 105 + G ++E LR +G+EI+ LT+L +LE FE A G V WA+DG E +++ +I Sbjct: 45 SVGQAGDFETLRGIGAEIRDTALTDLDAWLEAFEAKATATGATVLWARDGREAQQLIVDI 104 Query: 106 LASHKVKKLVKSKSMLTEECHLNPYLEQRGIEVIDTDLGERIIQLAKMPPSHIVVPAIHM 165 H VKK++KSKSML+EE LN LE G++ ++TDLGE I+QLAK PPSHI+ PAIH Sbjct: 105 AKRHGVKKVIKSKSMLSEEAGLNEGLEAAGVQSVETDLGEYILQLAKEPPSHILAPAIHK 164 Query: 166 KKEEVGDLF---HDKLGTKAGESDPLYLTRAARAHLREQFLSADAAMTGVNMAIADKGAV 222 KEEV +LF H + T G+ D LTR AR LRE FLSAD +TG N +A+ G+V Sbjct: 165 NKEEVDELFARCHGRPVTPEGQIDIPALTREARVALREHFLSADMGITGGNFLVAETGSV 224 Query: 223 VVCTNEGNADMGANLPKLQLHSMGIDKVVPDIDSAAVLLRTLARNATGQPVTTYSAFYRG 282 + TNEGN M LP++ + +GI+KV+P ++ + LLR L R+ATGQ ++ Y + G Sbjct: 225 ALVTNEGNGRMVTTLPRVHVAVVGIEKVIPTLEDLSALLRLLTRSATGQTISNYVSLLTG 284 Query: 283 PQVDG------EMHVIIVDNGRTEMMKDKILAESLKCIRCGGCLNTCPVYRRSGGYSYNY 336 P+ +G M+ +++DNGR ++ E L+CIRCG C+N CPVY+ GG++Y + Sbjct: 285 PRAEGAVEGPEHMYFVLMDNGRAGLVGGD-FQEMLRCIRCGACMNHCPVYQSIGGHAYGW 343 Query: 337 TIPGPIGIAVGATH---DNTNSIAWACTLCGSCTYVCPTKVPLDKIIHHHRRLKAEAGKL 393 PGP+G + + + + A TLCG C+ VCP K+PL +++ R + E Sbjct: 344 VYPGPMGSVLTPLYTGLEQAPDLPQAATLCGQCSIVCPVKIPLPELLRKLREKQMETELR 403 Query: 394 PYGKNAYMPLVGKFMASTTLLNCSMGAARTALRILPGSLLK----PFSGAWGKYRELPVA 449 P+ + + G F A L + G AL++L G P W + R+ P Sbjct: 404 PWQERWALRTWGFFAARPRLYALAAGLGARALKLLAGGKASIRTLPGVPEWSRGRDFPAP 463 Query: 450 PNSSFEAWFKKHR 462 +F + R Sbjct: 464 QGKTFRELYAARR 476 Lambda K H 0.320 0.134 0.413 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 500 Number of extensions: 24 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 464 Length of database: 479 Length adjustment: 33 Effective length of query: 431 Effective length of database: 446 Effective search space: 192226 Effective search space used: 192226 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory